Data / Medical devices / United States / Pourang Bral, DDS, LLC
Pourang Bral, DDS, LLC: FDA-registered device maker in Jersey City, NJ, United States, 1 510(k) clearance
Pourang Bral, DDS, LLC is registered with the FDA (registration 3006469120) in Jersey City, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 9, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006469120
- Address
- 901 Bergen Ave, Jersey City, NJ, United States, 07306
- Owner or operator
- Pourang Bral, DDS, LLC (10087606)
- Roles
- Manufacturer
- First device listed
- March 26, 2023
- Registered through
- 2026
- Brand names listed
- Noodle
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 9, 2022 | K220573 | Noodle | NUH | Substantially Equivalent | Pourang Bral, Dds, LLC | accessdata.fda.gov |
Compare with other makers
Updated July 9, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.